US5491024A - Photodegradable cellulose ester tow - Google Patents

Photodegradable cellulose ester tow Download PDF

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Publication number
US5491024A
US5491024A US08/404,477 US40447795A US5491024A US 5491024 A US5491024 A US 5491024A US 40447795 A US40447795 A US 40447795A US 5491024 A US5491024 A US 5491024A
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acetate
titanium dioxide
cellulose
cellulose ester
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US08/404,477
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Terry A. Brodof
John B. Hopkins, Jr.
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CNA Holdings LLC
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Hoechst Celanese Corp
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Assigned to HOECHST CELANESE CORPORATION ROUTE 202-206 NORTH SOMERVILLE, NJ 08876 reassignment HOECHST CELANESE CORPORATION ROUTE 202-206 NORTH SOMERVILLE, NJ 08876 ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: BRODOF, TERRY A., HOPKINS, JOHN B., JR.
Priority to US08/404,477 priority Critical patent/US5491024A/en
Application filed by Hoechst Celanese Corp filed Critical Hoechst Celanese Corp
Priority to US08/559,393 priority patent/US5647383A/en
Application granted granted Critical
Publication of US5491024A publication Critical patent/US5491024A/en
Priority to JP05111996A priority patent/JP3532689B2/en
Priority to EP96103843A priority patent/EP0732432B1/en
Priority to AT96103843T priority patent/ATE173305T1/en
Priority to DE69600936T priority patent/DE69600936T2/en
Priority to CNB961058005A priority patent/CN1135273C/en
Assigned to CNA HOLDINGS, INC. reassignment CNA HOLDINGS, INC. CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: HNA HOLDINGS, INC. (DE CORPORATION)
Assigned to HNA HOLDINGS, INC. reassignment HNA HOLDINGS, INC. CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: HOECHST CELANESE CORPORATION
Assigned to DEUTSCHE BANK AG, NEW YORK BRANCH reassignment DEUTSCHE BANK AG, NEW YORK BRANCH SECURITY AGREEMENT Assignors: CNA HOLDINGS, INC.
Assigned to DEUTSCHE BANK AG, NEW YORK BRANCH reassignment DEUTSCHE BANK AG, NEW YORK BRANCH SECURITY INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: CNA HOLDINGS, INC. (F/K/A/ HOECHST CELANESE CORPORATION AND HNA HOLDINGS, INC.)
Assigned to DEUTSCHE BANK AG, NEW YORK BRANCH, AS COLLATERAL AGENT reassignment DEUTSCHE BANK AG, NEW YORK BRANCH, AS COLLATERAL AGENT ASSIGNMENT OF SECURITY INTEREST IN CERTAIN PATENTS Assignors: CNA HOLDINGS, INC.
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Classifications

    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F2/00Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof
    • D01F2/24Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from cellulose derivatives
    • D01F2/28Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from cellulose derivatives from organic cellulose esters or ethers, e.g. cellulose acetate
    • AHUMAN NECESSITIES
    • A24TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24DCIGARS; CIGARETTES; TOBACCO SMOKE FILTERS; MOUTHPIECES FOR CIGARS OR CIGARETTES; MANUFACTURE OF TOBACCO SMOKE FILTERS OR MOUTHPIECES
    • A24D3/00Tobacco smoke filters, e.g. filter-tips, filtering inserts; Filters specially adapted for simulated smoking devices; Mouthpieces for cigars or cigarettes
    • A24D3/06Use of materials for tobacco smoke filters
    • A24D3/067Use of materials for tobacco smoke filters characterised by functional properties
    • A24D3/068Biodegradable or disintegrable
    • AHUMAN NECESSITIES
    • A24TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24DCIGARS; CIGARETTES; TOBACCO SMOKE FILTERS; MOUTHPIECES FOR CIGARS OR CIGARETTES; MANUFACTURE OF TOBACCO SMOKE FILTERS OR MOUTHPIECES
    • A24D3/00Tobacco smoke filters, e.g. filter-tips, filtering inserts; Filters specially adapted for simulated smoking devices; Mouthpieces for cigars or cigarettes
    • A24D3/06Use of materials for tobacco smoke filters
    • A24D3/08Use of materials for tobacco smoke filters of organic materials as carrier or major constituent
    • A24D3/10Use of materials for tobacco smoke filters of organic materials as carrier or major constituent of cellulose or cellulose derivatives
    • AHUMAN NECESSITIES
    • A24TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24DCIGARS; CIGARETTES; TOBACCO SMOKE FILTERS; MOUTHPIECES FOR CIGARS OR CIGARETTES; MANUFACTURE OF TOBACCO SMOKE FILTERS OR MOUTHPIECES
    • A24D3/00Tobacco smoke filters, e.g. filter-tips, filtering inserts; Filters specially adapted for simulated smoking devices; Mouthpieces for cigars or cigarettes
    • A24D3/06Use of materials for tobacco smoke filters
    • A24D3/16Use of materials for tobacco smoke filters of inorganic materials
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F1/00General methods for the manufacture of artificial filaments or the like
    • D01F1/02Addition of substances to the spinning solution or to the melt
    • D01F1/04Pigments
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/29Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2913Rod, strand, filament or fiber
    • Y10T428/2927Rod, strand, filament or fiber including structurally defined particulate matter
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/29Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2913Rod, strand, filament or fiber
    • Y10T428/2933Coated or with bond, impregnation or core
    • Y10T428/2964Artificial fiber or filament
    • Y10T428/2965Cellulosic

Definitions

  • This invention is directed to a photodegradable cellulose ester tow.
  • Cellulose ester tow is known. Kirk-Othmer, Encyclopedia of Chemical Technology, 4th Edition, Vol. 5, John Wiley & Sons, New York, N.Y., 1993, p. 496-529. Cellulose acetate tow is known. Kirk-Othmer, Encyclopedia of Chemical Technology, 3rd Edition, Vol. 5, John Wiley & Sons, New York, N.Y., 1979, p. 89-117. Cellulose acetate tow impregnated with titanium dioxide pigments, either anatase or rutile, as a delustrant is known. See: Kirk-Othmer, Ibid, 3rd Edition, p. 90; and U.S. Pat. No. 4,022,632.
  • the ideal delustering titanium dioxide pigment has a particle size ranging from 200 to 350 nm (0.2 to 0.35 microns). See: Undated publication of Kemira, Inc. entitled “The Savannah Story”. These pigments are typically coated to retard their photocatalytic effect. Rabek, J. F., Mechanisms of Photophysical Processes and Photochemical Reactions in Polymers, John Wiley & Sons, New York City, N.Y., 1987, p. 585-587.
  • anatase-type titanium dioxides can be used to accelerate the photodegradation of cellulose ester tows. See: EPO Publication No. 597,478; WO 93/24685; and U.S. Pat. No. 5,242,880. These photodegradable cellulose ester tows utilize uncoated anatases. Ibid. As a photodegradability accelerator, anatase-type titanium dioxide is better than rutile-type titanium dioxide. In EPO Publication No.
  • the cellulose ester tow has about 0-5% by weight of an anatase-type titanium dioxide having an average particle diameter of about 300 nm (0.3 microns), a particle size distribution of 10-1000 nm (0.01-1 micron), and specific surface area of 3 to 30 m 2 /g.
  • the average particle size is given by reference to the exemplary photoactive anatase titanium dioxides set forth in Table 1 at page 48. Therein, three commercially available pigments are disclosed. Each is believed to have an average particle size of about 350 nm (0.35 microns).
  • an oxidizable polymer such as cellulose acetate or polypropylene
  • a photoactive catalyst to increase biodegradability.
  • the photoactive catalyst comprises an anatase-type titanium dioxide containing or coated with a salt.
  • the salt comprises between 2-30 weight percent of the catalyst.
  • Fine particle, crystalline titanium dioxides (8-210 nm or 0.008-0.210 micron) are known for use as photodegradants in plastics. See: Meldrum, B. J., "Fine Particle TiO 2 --A Brief Introduction", SPE 49th Annual Technical Conference Exhibits, 1991. Therein, uncoated, fine particles of titanium dioxide are loaded into polypropylene film which is then exposed to ultraviolet radiation, so to demonstrate the photodegradation effect.
  • the present invention is directed to a man-made fiber comprising a cellulose ester and 0.05 to 5.0% by weight of a titanium dioxide having an average particle size of less than 100 nanometers (nm) .
  • the invention is a man-made fiber comprising a cellulose ester and 0.05 to 5.0% by weight of a titanium dioxide having an average particle size of less than 100 nanometers.
  • a cellulose ester is a cellulose acetate, having a degree of substitution of 1.5 to 2.7
  • the preferred weight range of titanium dioxide is 0.1 to 3.0%.
  • These man-made fibers are adapted to photodegrade. Cellulose acetate fibers, having a degree of substitution 1.5 to 2.7, will substantially degrade in 300 hours or less.
  • the basis for measuring "substantial degradation" is AATCC TEST METHOD 169-1990 as discussed in greater detail below.
  • substantial degradation refers to a tenacity of less than or equal to 0.2 grams/denier at 200 hours.
  • Cellulose ester refers to organic esters. Examples of such esters include: cellulose acetate; cellulose propionate; cellulose butyrate; cellulose acetate propionate; cellulose acetate butyrate; cellulose propionate butyrate; and the like; and combinations thereof.
  • the cellulose esters useful in the present invention can be prepared by any known technique. See: Kirk-Othmer, Encyclopedia of Chemical Technology, 3rd Edition, Vol. 5, John Wiley & Sons, New York, N.Y., 1979, p. 89-129; and Libscomb, A. G., Cellulose Acetate: Its Manufacture and Applications, Ernest Benn, Ltd. London, GB, 1933, both are incorporated herein by reference.
  • the cellulose esters of the present invention preferably have at least 2 anhydroglucose rings and most preferably have about 2 and 5,000 anhydroglucose rings.
  • such polymers typically have an inherent viscosity (IV) of about 0.2 to about 3.0 deciliters per gram, most preferably about 1 to 1.6, as measured at a temperature of 25° C. from a 0.5 gram sample and 100 ml of a 60/40 by weight solution of phenol/tetrachloroethane.
  • IV inherent viscosity
  • the DS/AGU (degree of substitution per anhydroglycose unit) of the cellulose esters useful herein ranges from about 1.5 to about 2.7.
  • Cellulose acetates having a DS/AGU of 1.7 to 2.6 are especially preferred.
  • the most preferred cellulose acetate has a DS/AGU of 1.8 to 2.2 and an IV of 1.3 to 1.5.
  • any known, conventional additives to cellulose ester tow maybe incorporated into the inventive tows set forth herein.
  • delustrants e.g., titanium dioxide
  • spin finishes may be added, as is well known.
  • Titanium dioxide refers to any titanium dioxide material having an average particle size less than 100 nanometers. These titanium dioxides may also have a specific surface area of greater than 50 m 2 /g. Materials of this type are commercially available from: Sachtleben Chemie GmbH, Duisburg, Germany under the trade name "HOMBIFINE N”; Kemira Group, Pori, Finland under the tradename "UV-Titan”; Ishihara Corporation, San Francisco, Calif., U.S.A. under the tradename TIPAQUE® titanium dioxide TTO-55 and TTO-51 Series; Tioxide Chemicals Ltd., Billingham, Cleveland, Great Britain under the trade designation of "UF”.
  • the titanium dioxide is an uncoated anatase material having an average particle size less 10 nanometers and a specific surface are of about 250 m 2 /g.
  • Uncoated refers to the absence of the coatings of inorganic materials used to retard the photocatalytic effect of many commercial titanium dioxides. See: Rabek, J., Ibid., p. 257-259, incorporated herein by reference.
  • Such inorganic coatings include, without limit: alumina, silica, zinc oxide, manganese acetate, silver acetate, thallium acetate, gallium acetate, ferric acetate, lead acetate, rubidium acetate, strontium acetate, aluminum acetate, lanthanum acetate, zirconium acetate, uranyl acetate, potassium acetate, samarium acetate, praseodymium acetate, niobium acetate, neodymium acetate, cupric acetate, magnesium acetate, barium acetate, yttrium acetate, sodium acetate, lithium acetate, chromic acetate, stannous acetate, didymium acetate, nikelous acetate, calcium acetate, cerous acetate, zinc acetate, cobaltous acetate, and manganous acetate.
  • the titanium dioxide is added to the "dope" (i.e., the solvated cellulose ester) prior to extrusion into the tow. Addition of the titanium dioxide may be at any convenient point prior to extrusion. No special preparation of the titanium dioxide is required, except that one should insure that agglomeration of the fine particles is minimized or reduced so that the photoactivity provided by the fine particles is maximized. Extrusion of the tow maybe accomplished, as is well known, in any conventional manner. See: Browne, C. L., The Design of Cigarettes, Hoechst Celanese Corporation, Charlotte, N.C., 1990, p. 59-64, incorporated herein by reference.
  • Cigarette refers to any commonly known cigarette comprising a tobacco column and a filter as those terms are commonly used in the industry. See: Browne, C. L., The Design of Cigarettes, Hoechst Celanese Corporation, Charlotte, N.C., 1990, incorporated herein by reference.
  • the yarns are evaluated according to the procedures of the American Association of Textile Chemist and Colorists (AATCC).
  • AATCC Test Method 169-1990 "Weather Resistance of Textiles: Xenon Lamp Exposure", Option 1 is used.
  • Yarns are prepared for evaluation according to AATCC Test Method 177-1993 "Colorfastness to Light at Elevated Temperature and Humidity: Water Cooled Xenon Lamp Apparatus".
  • the yarns are wrapped around a paper card and placed in a metal holder.
  • Theholder with the yarn is placed in an Atlas model C65 WeatherOmeter and subjected to alternating conditions of Xenon light exposure and water spray.
  • Conditions (option 1) have been predetermined to equate to environmental conditions of South Florida.
  • yarns are removed, conditioned to ambient conditions and then breaking strength is measured.
  • Kemira 0-310 pigment grade Ti02 (anatase) with a median diameter of 420 nm.

Abstract

The present invention is directed to a man-made fiber comprising a cellulose ester and 0.05 to 5.0% by weight of a titanium dioxide having an average particle size of less than 100 nanometers.

Description

FIELD OF THE INVENTION
This invention is directed to a photodegradable cellulose ester tow.
BACKGROUND OF THE INVENTION
Cellulose ester tow is known. Kirk-Othmer, Encyclopedia of Chemical Technology, 4th Edition, Vol. 5, John Wiley & Sons, New York, N.Y., 1993, p. 496-529. Cellulose acetate tow is known. Kirk-Othmer, Encyclopedia of Chemical Technology, 3rd Edition, Vol. 5, John Wiley & Sons, New York, N.Y., 1979, p. 89-117. Cellulose acetate tow impregnated with titanium dioxide pigments, either anatase or rutile, as a delustrant is known. See: Kirk-Othmer, Ibid, 3rd Edition, p. 90; and U.S. Pat. No. 4,022,632. The ideal delustering titanium dioxide pigment has a particle size ranging from 200 to 350 nm (0.2 to 0.35 microns). See: Undated publication of Kemira, Inc. entitled "The Savannah Story". These pigments are typically coated to retard their photocatalytic effect. Rabek, J. F., Mechanisms of Photophysical Processes and Photochemical Reactions in Polymers, John Wiley & Sons, New York City, N.Y., 1987, p. 585-587.
It has been proposed that anatase-type titanium dioxides can be used to accelerate the photodegradation of cellulose ester tows. See: EPO Publication No. 597,478; WO 93/24685; and U.S. Pat. No. 5,242,880. These photodegradable cellulose ester tows utilize uncoated anatases. Ibid. As a photodegradability accelerator, anatase-type titanium dioxide is better than rutile-type titanium dioxide. In EPO Publication No. 597,478, the cellulose ester tow has about 0-5% by weight of an anatase-type titanium dioxide having an average particle diameter of about 300 nm (0.3 microns), a particle size distribution of 10-1000 nm (0.01-1 micron), and specific surface area of 3 to 30 m2 /g. In WO 93/24685, the average particle size is given by reference to the exemplary photoactive anatase titanium dioxides set forth in Table 1 at page 48. Therein, three commercially available pigments are disclosed. Each is believed to have an average particle size of about 350 nm (0.35 microns). In U.S. Pat. No. 5,242,880, an oxidizable polymer such as cellulose acetate or polypropylene, is impregnated with a photoactive catalyst to increase biodegradability. The photoactive catalyst comprises an anatase-type titanium dioxide containing or coated with a salt. The salt comprises between 2-30 weight percent of the catalyst.
Fine particle, crystalline titanium dioxides (8-210 nm or 0.008-0.210 micron) are known for use as photodegradants in plastics. See: Meldrum, B. J., "Fine Particle TiO2 --A Brief Introduction", SPE 49th Annual Technical Conference Exhibits, 1991. Therein, uncoated, fine particles of titanium dioxide are loaded into polypropylene film which is then exposed to ultraviolet radiation, so to demonstrate the photodegradation effect.
There is a need for photodegradable cellulose ester tows that can minimize the littering problem associated with the disposal of spent cigarettes, having filters made from cellulose esters tows, on roadsides and the like.
SUMMARY OF THE INVENTION
The present invention is directed to a man-made fiber comprising a cellulose ester and 0.05 to 5.0% by weight of a titanium dioxide having an average particle size of less than 100 nanometers (nm) .
DETAILED DESCRIPTION OF THE INVENTION
The present invention is described in greater detail below.
The invention is a man-made fiber comprising a cellulose ester and 0.05 to 5.0% by weight of a titanium dioxide having an average particle size of less than 100 nanometers. When the cellulose ester is a cellulose acetate, having a degree of substitution of 1.5 to 2.7, the preferred weight range of titanium dioxide is 0.1 to 3.0%. These man-made fibers are adapted to photodegrade. Cellulose acetate fibers, having a degree of substitution 1.5 to 2.7, will substantially degrade in 300 hours or less. The basis for measuring "substantial degradation" is AATCC TEST METHOD 169-1990 as discussed in greater detail below. Preferably, substantial degradation refers to a tenacity of less than or equal to 0.2 grams/denier at 200 hours.
Cellulose ester refers to organic esters. Examples of such esters include: cellulose acetate; cellulose propionate; cellulose butyrate; cellulose acetate propionate; cellulose acetate butyrate; cellulose propionate butyrate; and the like; and combinations thereof. The cellulose esters useful in the present invention can be prepared by any known technique. See: Kirk-Othmer, Encyclopedia of Chemical Technology, 3rd Edition, Vol. 5, John Wiley & Sons, New York, N.Y., 1979, p. 89-129; and Libscomb, A. G., Cellulose Acetate: Its Manufacture and Applications, Ernest Benn, Ltd. London, GB, 1933, both are incorporated herein by reference. The cellulose esters of the present invention preferably have at least 2 anhydroglucose rings and most preferably have about 2 and 5,000 anhydroglucose rings. Also, such polymers typically have an inherent viscosity (IV) of about 0.2 to about 3.0 deciliters per gram, most preferably about 1 to 1.6, as measured at a temperature of 25° C. from a 0.5 gram sample and 100 ml of a 60/40 by weight solution of phenol/tetrachloroethane. In addition, the DS/AGU (degree of substitution per anhydroglycose unit) of the cellulose esters useful herein ranges from about 1.5 to about 2.7. Cellulose acetates having a DS/AGU of 1.7 to 2.6 are especially preferred. The most preferred cellulose acetate has a DS/AGU of 1.8 to 2.2 and an IV of 1.3 to 1.5.
Any known, conventional additives to cellulose ester tow maybe incorporated into the inventive tows set forth herein. For example, delustrants (e.g., titanium dioxide) and spin finishes may be added, as is well known.
Titanium dioxide, as used herein, refers to any titanium dioxide material having an average particle size less than 100 nanometers. These titanium dioxides may also have a specific surface area of greater than 50 m2 /g. Materials of this type are commercially available from: Sachtleben Chemie GmbH, Duisburg, Germany under the trade name "HOMBIFINE N"; Kemira Group, Pori, Finland under the tradename "UV-Titan"; Ishihara Corporation, San Francisco, Calif., U.S.A. under the tradename TIPAQUE® titanium dioxide TTO-55 and TTO-51 Series; Tioxide Chemicals Ltd., Billingham, Cleveland, Great Britain under the trade designation of "UF".
Preferably, the titanium dioxide is an uncoated anatase material having an average particle size less 10 nanometers and a specific surface are of about 250 m2 /g. Uncoated refers to the absence of the coatings of inorganic materials used to retard the photocatalytic effect of many commercial titanium dioxides. See: Rabek, J., Ibid., p. 257-259, incorporated herein by reference. Such inorganic coatings include, without limit: alumina, silica, zinc oxide, manganese acetate, silver acetate, thallium acetate, gallium acetate, ferric acetate, lead acetate, rubidium acetate, strontium acetate, aluminum acetate, lanthanum acetate, zirconium acetate, uranyl acetate, potassium acetate, samarium acetate, praseodymium acetate, niobium acetate, neodymium acetate, cupric acetate, magnesium acetate, barium acetate, yttrium acetate, sodium acetate, lithium acetate, chromic acetate, stannous acetate, didymium acetate, nikelous acetate, calcium acetate, cerous acetate, zinc acetate, cobaltous acetate, and manganous acetate.
The titanium dioxide is added to the "dope" (i.e., the solvated cellulose ester) prior to extrusion into the tow. Addition of the titanium dioxide may be at any convenient point prior to extrusion. No special preparation of the titanium dioxide is required, except that one should insure that agglomeration of the fine particles is minimized or reduced so that the photoactivity provided by the fine particles is maximized. Extrusion of the tow maybe accomplished, as is well known, in any conventional manner. See: Browne, C. L., The Design of Cigarettes, Hoechst Celanese Corporation, Charlotte, N.C., 1990, p. 59-64, incorporated herein by reference.
Cigarette, is used herein, refers to any commonly known cigarette comprising a tobacco column and a filter as those terms are commonly used in the industry. See: Browne, C. L., The Design of Cigarettes, Hoechst Celanese Corporation, Charlotte, N.C., 1990, incorporated herein by reference.
EXAMPLE
All yarn were prepared in a conventional manner. See: Cellulose Chemistry And Its Applications, Ellis Harwood Ltd., Chichester, England, 1985, p. 474-476, incorporated herein by reference. Cellulose acetate polymer is dissolved in a solvent of 96% acetone and 4% water. In all cases, 100 lbs of total solution prepared which contained 27 lbs of cellulose acetate polymer in 73 pounds of a 96%/4% acetone/water solvent. If titanium dioxide is added, it is done so after the polymer is dissolved in the solvent. The mixture is stirred until homogenous, and filtered. After filtering, yarn is extruded through a 190 hole spinnerette with a hole diameter of 52 μm. This results in a fiber with 2.9 denier/filament.
The yarns are evaluated according to the procedures of the American Association of Textile Chemist and Colorists (AATCC). AATCC Test Method 169-1990 "Weather Resistance of Textiles: Xenon Lamp Exposure", Option 1 is used. Yarns are prepared for evaluation according to AATCC Test Method 177-1993 "Colorfastness to Light at Elevated Temperature and Humidity: Water Cooled Xenon Lamp Apparatus".
The yarns are wrapped around a paper card and placed in a metal holder. Theholder with the yarn is placed in an Atlas model C65 WeatherOmeter and subjected to alternating conditions of Xenon light exposure and water spray. Conditions (option 1) have been predetermined to equate to environmental conditions of South Florida. At 100 hours intervals, which roughly relate to one month outdoors exposure, yarns are removed, conditioned to ambient conditions and then breaking strength is measured.
Example 1
Yarn prepared as described above with the addition of 0.135 lbs of Kemira 0-310 pigment grade Ti02 (anatase) with a median diameter of 420 nm.
Example 2
Yarn prepared as described above with no added Ti02.
Example 3
Yarn prepared as described above with the addition of 0.135 lbs of Kemira 0-310 Ti02 (Anatase) plus 0.135 lbs of Hombifine N ultra fine grind Ti02 (Anatase) with a primary particle diameter of less than 10 nm.
Example 4
Yarn prepared as described above with the addition of 0.135 lbs of Hombifine N Ti02.
Example 5
Yarn prepared as described above with the addition of 0.27 lbs. of Hombifine N Ti02.
As Table 1 shows, yarns prepared with ultra fine Ti02, Examples 3, 4, and 5disintegrate (breaking strength=0 grams/denier) quicker than yarns preparedwith pigment grade Ti02, Example 1 or no Ti02 at all, Example 2. Even though Examples 3 and 4 both contained the same amount of ultra fine grindTi02, Example 3, which also contained pigment grade Ti02, disintegrated slower that Example 4 which only contained the ultra fine grind Ti02. Thisis due to the light refractive characteristics of pigment grade Ti02.
              TABLE 1                                                     
______________________________________                                    
Tenacity (grams/denier) of various CA                                     
yarns exposed in the weatherometer                                        
                   0      100     200  300                                
SAMPLE             Hrs    Hrs     Hrs  Hrs                                
______________________________________                                    
Example 1          1.06   0.79    0.54 0.15                               
0.5% PIGMENT GRADE TiO2                                                   
Example 2          1.14   0.68    0.53 0.14                               
0.0% TiO2                                                                 
Example 3          1.06   0.46    0.14 0                                  
0.5% ULTRA FINE TiO2                                                      
0.5% PIGMENT GRADE TiO2                                                   
Example 4          1.08   0.55    0.06 0                                  
0.5% ULTRA FINE TiO2                                                      
Example 5          1.05   0.28    0    0                                  
1.0% ULTRA FINE TiO2                                                      
______________________________________                                    

Claims (4)

We claim:
1. A man-made fiber comprising a mixture of:
a cellulose ester; and
about 0.05 to 5.0% by weight of titanium dioxide having an average particle size of less than 100 nanometers.
2. A man-made fiber comprising a mixture of:
a cellulose acetate having a degree of substitution of 1.5 to 2.7;
about 0.05 to 5.0% by weight of titanium dioxide having an average particle size of less than 100 nanometers; and being adapted to be substantially degraded, as measured by AATCC TEST METHOD 169-1990, in 300 hours or less.
3. The fiber according to claim 2 wherein said titanium dioxide in said cellulose acetate ranges from about 0.1 to 3.0% by weight.
4. The fiber according to claim 2 wherein substantially degraded means a tenacity of less than or equal to 0.2 grams/denier at 200 hours.
US08/404,477 1995-03-14 1995-03-14 Photodegradable cellulose ester tow Expired - Lifetime US5491024A (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
US08/404,477 US5491024A (en) 1995-03-14 1995-03-14 Photodegradable cellulose ester tow
US08/559,393 US5647383A (en) 1995-03-14 1995-11-15 Photodegradable cellulose ester tow
JP05111996A JP3532689B2 (en) 1995-03-14 1996-03-08 Photodegradable cellulose ester fiber bundle
EP96103843A EP0732432B1 (en) 1995-03-14 1996-03-12 Photodegradable cellulose ester tow
AT96103843T ATE173305T1 (en) 1995-03-14 1996-03-12 PHOTODEGRADABLE CELLULOSE ESTERNAL STRAND
DE69600936T DE69600936T2 (en) 1995-03-14 1996-03-12 Photo-degradable cellulose ester strand
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US20090151738A1 (en) * 2007-12-17 2009-06-18 Celanese Acetate Llc Degradable cigarette filter
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US7878210B2 (en) 2007-06-04 2011-02-01 Philip Morris Usa Inc. Cellulose acetate fiber modification
US20110143067A1 (en) * 2008-08-14 2011-06-16 Hoelter Dirk Photodegradable plastic and its use
EP2357277A1 (en) 2010-02-12 2011-08-17 Rhodia Acetow GmbH Photodegradable paper and its use
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US5728462A (en) * 1994-02-04 1998-03-17 Daicel Chemical Industries, Ltd. Cigarette filter material
US5856006A (en) * 1994-09-19 1999-01-05 Daicel Chemical Industries, Ltd. Tobacco filter material and a method for producing the same
EP0880907A2 (en) 1997-05-29 1998-12-02 Eastman Chemical Company Environmentally disintegratable tobacco smoke filter rod and method for producing same
US6571802B1 (en) 1998-03-31 2003-06-03 Japan Tobacco Inc. Molded article of biodegradable cellulose acetate and filter plug for smoking article
JP2011032629A (en) * 2004-06-25 2011-02-17 Celanese Acetate Llc Cigarette filter tow, cigarette filter rod, cigarette filter chip and cigarette
US6924029B1 (en) * 2004-06-25 2005-08-02 Celanese Acetate, Llc Cellulose acetate tow and method of making same
WO2006007020A1 (en) * 2004-06-25 2006-01-19 Celanese Acetate Llc Cellulose acetate tow and method of making same
KR100845011B1 (en) 2004-06-25 2008-07-09 셀라네세 아세테이트 앨앨씨 Cellulose acetate tow and method of making same
CN100491607C (en) * 2004-06-25 2009-05-27 赛拉尼斯醋酸盐有限公司 Cellulose acetate tow and method of making same
CN101422281B (en) * 2004-06-25 2012-06-20 赛拉尼斯醋酸盐有限公司 Cellulose acetate tow and method of making same
US20050283959A1 (en) * 2004-06-25 2005-12-29 Caenen Philip I L Cellulose acetate tow and method of making same
US7585442B2 (en) 2004-06-25 2009-09-08 Celanese Acetate, Llc Process for making cellulose acetate tow
US7878210B2 (en) 2007-06-04 2011-02-01 Philip Morris Usa Inc. Cellulose acetate fiber modification
KR101135403B1 (en) * 2007-07-03 2012-04-17 타이유 켄세츠 카부시키카이샤 Process for production of monosaccharide and process for production of ethanol both utilizing cellulose-based substance
WO2009079202A1 (en) 2007-12-17 2009-06-25 Celanese Acetate Llc Degradable cigarette filter
US9155335B2 (en) 2007-12-17 2015-10-13 Celanese Acetate Llc Degradable cigarette filter
US20090151738A1 (en) * 2007-12-17 2009-06-18 Celanese Acetate Llc Degradable cigarette filter
US8697213B2 (en) 2008-08-14 2014-04-15 Solvay Acetow Gmbh Photodegradable plastics material and its use
US20110143067A1 (en) * 2008-08-14 2011-06-16 Hoelter Dirk Photodegradable plastic and its use
RU2519929C2 (en) * 2008-08-14 2014-06-20 Родиа Ацетов Гмбх Photodegradable synthetic material and use thereof
EP2357277A1 (en) 2010-02-12 2011-08-17 Rhodia Acetow GmbH Photodegradable paper and its use
WO2011098510A1 (en) 2010-02-12 2011-08-18 Rhodia Acetow Gmbh Photodegradable paper and its use
US8986502B2 (en) 2010-02-12 2015-03-24 Solvay Acetow Gmbh Photodegradable paper and its use
CN101862037A (en) * 2010-05-28 2010-10-20 华南理工大学 Preparation method and application of hexagonal mesoporous monox coated nano-TiO2 composite material
CN101862037B (en) * 2010-05-28 2012-05-09 华南理工大学 Preparation method and application of hexagonal mesoporous monox coated nano-TiO2 composite material
WO2012177483A1 (en) 2011-06-23 2012-12-27 Eastman Chemical Company Cellulose esters having mixed-phase titanium dioxide particles for improved degradation
WO2012177482A1 (en) 2011-06-23 2012-12-27 Eastman Chemical Company Filters having improved degradation and methods of making them
JP2016528037A (en) * 2013-08-12 2016-09-15 ソルベイ アセトウ ゲーエムベーハー Method for producing a product containing a catalytically active titanium compound

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